Damascus Bakery, Bantam Classic Bagels, 6/1.3 oz pieces per carton (7.8 oz), Paper Carton .
Summary
The FDA issued a Class II for Damascus Bakery, Bantam Classic Bagels, 6/1.3 oz pieces per carton (7.8 oz), Pap by Damascus Bakery LLC. Reason: Undeclared Egg Allergen.
Details
Source
Food Recall
External ID
F-0899-2022
Action Date
2022-03-30
Status
Terminated
Category
food
Product Description
Damascus Bakery, Bantam Classic Bagels, 6/1.3 oz pieces per carton (7.8 oz), Paper Carton .
Lot/Code Info: Product Code -Classic Bagels- 213455 Lot Code BB May/27/2023
Quantity Affected: 232 cases
Reason for Recall
Undeclared Egg Allergen
Distribution
The product was distributed to the following states: SC, PA, MA, MN, NY, IN.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-25
Company
Newark, NJ
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 52 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Damascus Bakery LLC has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Damascus Bakery LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Damascus Bakery LLC have FDA actions?
Damascus Bakery LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0899-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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